Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756207760
CXCR4
2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs731580
FGD5
3 14815331 intron variant G/A snv 0.31 2
rs1552896
FREM1
9 14841389 intron variant C/A;G snv 1
rs11087114
MACROD2-AS1 ; MACROD2
20 14931037 intron variant G/A;C snv 1
rs9648724
PRKAG2 ; LOC644090
7 151805216 intron variant G/A snv 0.21 1
rs6909587
LOC101928923 ; LOC105378072
6 155880114 intergenic variant C/T snv 0.78 1
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs396716
FCGR3A
1 161544806 missense variant A/G snv 7.2E-05 6.3E-05 1
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs2243191
LOC105372878 ; IL19
1.000 0.040 1 206842612 missense variant T/C;G snv 0.71; 5.5E-06 2
rs7696218
PACRGL
4 20721189 intron variant G/A snv 0.11 2
rs11012476
NEBL
0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs201565523
SLC11A1
0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 3
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs17862875
UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7
2 233740656 intron variant G/A snv 0.30 4
rs34352510
UGT1A9 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A4
2 233741916 non coding transcript exon variant T/C snv 0.33 2
rs17864701
UGT1A4 ; UGT1A3 ; UGT1A6 ; UGT1A8 ; UGT1A7 ; UGT1A5 ; DNAJB3 ; UGT1A9 ; UGT1A10
2 233744071 intron variant C/T snv 0.30 3
rs11695484
DNAJB3 ; UGT1A3 ; UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A5
2 233745803 intron variant A/G snv 0.30 3
rs11888459
UGT1A8 ; UGT1A5 ; UGT1A2P ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A9
2 233747994 non coding transcript exon variant T/C snv 0.37 4
rs10178992
UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6
2 233749231 intron variant T/A snv 0.37 4
rs10179091
UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233749337 intron variant T/C snv 0.49 4
rs7604115
UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A4
2 233749470 intron variant C/T snv 0.37 4